Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initially.
Mimicry
Mitochondrial disease
Neuroinflammation
Treatment
Whole exome sequencing
Journal
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
ISSN: 1532-2130
Titre abrégé: Eur J Paediatr Neurol
Pays: England
ID NLM: 9715169
Informations de publication
Date de publication:
Nov 2022
Nov 2022
Historique:
received:
10
07
2022
revised:
05
09
2022
accepted:
15
09
2022
pubmed:
27
9
2022
medline:
7
12
2022
entrez:
26
9
2022
Statut:
ppublish
Résumé
Neuroimmunological diseases such as autoimmune encephalitis (AE) or acquired demyelinating syndromes (ADS), can present with neurological symptoms and imaging features that are indistinguishable from mitochondrial diseases (MD) in particular at initial presentation. Retrospective analysis of the clinical, laboratory and neuroimaging features of five patients who presented with signs of a neuroimmunological disease but all had pathological pathogenic variants in genes related to mitochondrial energy metabolism. Four patients presented with an acute neurological episode reminiscent of a possible AE and one patient with a suspected ADS at initial presentation. MRI findings were compatible with neuroimmunological diseases in all patients. In two children cerebrospinal fluid (CSF) studies revealed a mildly elevated cell count, two had elevated CSF lactate, none had oligoclonal bands (OCBs). All patients improved rapidly with intravenous steroids or immunoglobulins. Four patients had one or more relapses. Three patients showed worsening of their neurological symptoms with subsequent episodes and one patient died. Relapses in conjunction with new and progressive neurological symptoms, led to additional work-up which finally resulted in different genetic diagnosis of MD in all patients (MT-TL1, MT-ND5, APOA1-BP, HPDL, POLG). We would like to draw attention to a subset of patients with MD initially presenting with signs and symptoms mimicking neuroimmunological. Absence of CSF pleocytosis, elevated CSF lactate and progressive, relapsing course should trigger further (genetic) investigations in search of a MD even in patients with good response initially to immunomodulating therapies.
Identifiants
pubmed: 36162141
pii: S1090-3798(22)00138-6
doi: 10.1016/j.ejpn.2022.09.003
pii:
doi:
Substances chimiques
Steroids
0
Lactates
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
27-35Informations de copyright
© 2022 Published by Elsevier Ltd on behalf of European Paediatric Neurology Society.
Déclaration de conflit d'intérêts
Declaration of competing interest A. Blaschek, Wegener-Panzer, A. Della-Marina, M. Flotats-Bastardas, T. Reinhardt, I. El Naggar, F Distelmaier, U. Schara-Schmidt, S. Wortmann, Theresa Brunet, Matia Wagner, Dimitri Smirnov, Holger Prokisch have no disclosures. K. Rostásy received speaker's honoraria from Merck and served on the advisory board of the PARADIGM study.